ClinVar Miner

Variants in gene SLC25A15 with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
170 14 2 4 12 0 2 19

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 2 4 1 0 0
likely pathogenic 4 0 1 0 0
uncertain significance 1 1 0 11 1
likely benign 0 0 11 0 0
benign 0 0 1 0 0

All variants with conflicting interpretations #

Total variants: 19
Download table as spreadsheet
NM_014252.4(SLC25A15):c.147C>G (p.Asp49Glu) rs187685447
NM_014252.4(SLC25A15):c.182G>A (p.Arg61His) rs34615430
NM_014252.4(SLC25A15):c.216C>T (p.Ile72=) rs572717478
NM_014252.4(SLC25A15):c.225C>T (p.Ile75=) rs765380976
NM_014252.4(SLC25A15):c.255C>T (p.Tyr85=) rs536354947
NM_014252.4(SLC25A15):c.278G>A (p.Arg93Gln) rs369201060
NM_014252.4(SLC25A15):c.337G>A (p.Gly113Ser)
NM_014252.4(SLC25A15):c.345C>T (p.Phe115=) rs35434090
NM_014252.4(SLC25A15):c.388G>A (p.Val130Met) rs553432772
NM_014252.4(SLC25A15):c.446del (p.Ser149fs) rs1566123619
NM_014252.4(SLC25A15):c.564C>G (p.Phe188Leu) rs141028076
NM_014252.4(SLC25A15):c.564C>T (p.Phe188=) rs141028076
NM_014252.4(SLC25A15):c.565G>A (p.Gly189Ser) rs151239794
NM_014252.4(SLC25A15):c.658G>A (p.Gly220Arg) rs202247805
NM_014252.4(SLC25A15):c.706A>G (p.Arg236Gly) rs142236568
NM_014252.4(SLC25A15):c.815C>T (p.Thr272Ile) rs121908535
NM_014252.4(SLC25A15):c.823C>T (p.Arg275Ter) rs202247807
NM_014252.4(SLC25A15):c.824G>A (p.Arg275Gln) rs104894431
NM_014252.4(SLC25A15):c.861C>T (p.Tyr287=) rs148422923

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